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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669333Generated: November 1, 2026

Water → 1-(4'-Trifluoromethyl-biphenyl-4-yl)-heptan-1-ol

https://huagongshe.com/reaction/1669333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
Reactant4'-(Trifluoromethyl)-4-biphenylcarbaldehydeHCID 2782712—
ReactantHCID 178444609HCID 178444609—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(4'-Trifluoromethyl-biphenyl-4-yl)-heptan-1-olHCID 5972941373%

Reaction Steps

Add hexyl magnesium bromide (2.0M in ethyl ether, 8 mL, 16 mmol) to 4′-trifluoromethyl-biphenyl-4-carbaldehyde (2.0 g, 8 mmol) (prepared in a manner substantially similar to preparation 25, or other methods known in the art) in tetrahydro-furan (30 mL) at 0° C. under inert atmosphere. Stir 1.5 hours. Quench reaction with saturated solution of ammonium chloride, dilute with ethyl acetate. Wash organic phase with water then saturated sodium chloride solution. Dry organic fraction with Na2SO4, filter, and concentrate under reduced pressure. Purify on silica gel chromatography (0-30% Ethyl acetate/hexanes gradient) to provide 1.95 g of title compound (73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989457B2
Source datasetuspto-grants-2011_08
ORD IDord-d8c67ec133334ab4a89ec726ce5197cb
Source noteuspto-grants-2011_08